Physiological induction and reversal of focus formation and tumorigenicity in NIH 3T3 cells.
about
Activation of 5-HT1A receptors expressed in NIH-3T3 cells induces focus formation and potentiates EGF effect on DNA synthesisIncipient and overt stages of neoplastic transformationDegrees and kinds of selection in spontaneous neoplastic transformation: an operational analysisTransformation of BALB/c-3T3 cells: I. Investigation of experimental parameters that influence detection of spontaneous transformation.Cellular epigenetics: topochronology of progressive "spontaneous" transformation of cells under growth constraint.Selective nature of phorbol 12-myristate 13-acetate-induced neoplastic transformation in NIH 3T3 cells.Experimental control of neoplastic progression in cell populations: Foulds' rules revisited.A critical test of the role of population density in producing transformation.A novel canine kidney cell line model for the evaluation of neoplastic development: karyotype evolution associated with spontaneous immortalization and tumorigenicity.Clonal dynamics of progressive neoplastic transformationCell-cell contact interactions conditionally determine suppression and selection of the neoplastic phenotype.Automatic enumeration and characterization of heterogeneous clonal progression in cell transformation.Cellular epigenetics: effects of passage history on competence of cells for "spontaneous" transformation.Adaptive evolution of degrees and kinds of neoplastic transformation in cell culturePromotion and selection by serum growth factors drive field cancerization, which is anticipated in vivo by type 2 diabetes and obesityCoculturing diverse clonal populations prevents the early-stage neoplastic progression that occurs in the separate clonesSensitivity of transformation to small differences in population density during serial passage of NIH 3T3 cells.The cellular ecology of progressive neoplastic transformation: a clonal analysis.Irreversibility of cellular aging and neoplastic transformation: a clonal analysis.High rate of diversification and reversal among subclones of neoplastically transformed NIH 3T3 clones.Growth in high serum concentrations leads to rapid deadaptation of cells previously adapted to growth in an extremely low concentration of serum.CDK-inhibitor independent cell cycle progression in an experimental haematopoietic stem cell leukaemia despite unaltered Rb-phosphorylationThe nature of cancer: morphogenesis and progressive (self)-disorganization in neoplastic development and progression.Dynamics of cell transformation in culture and its significance for tumor development in animals.Phenotypic selection as the biological mode of epigenetic conversion and reversion in cell transformation.
P2860
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P2860
Physiological induction and reversal of focus formation and tumorigenicity in NIH 3T3 cells.
description
1990 nî lūn-bûn
@nan
1990 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1990 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
1990年の論文
@ja
1990年論文
@yue
1990年論文
@zh-hant
1990年論文
@zh-hk
1990年論文
@zh-mo
1990年論文
@zh-tw
1990年论文
@wuu
name
Physiological induction and re ...... morigenicity in NIH 3T3 cells.
@ast
Physiological induction and re ...... morigenicity in NIH 3T3 cells.
@en
type
label
Physiological induction and re ...... morigenicity in NIH 3T3 cells.
@ast
Physiological induction and re ...... morigenicity in NIH 3T3 cells.
@en
prefLabel
Physiological induction and re ...... morigenicity in NIH 3T3 cells.
@ast
Physiological induction and re ...... morigenicity in NIH 3T3 cells.
@en
P2093
P2860
P356
P1476
Physiological induction and re ...... morigenicity in NIH 3T3 cells.
@en
P2093
P2860
P304
10005-10009
P356
10.1073/PNAS.87.24.10005
P407
P577
1990-12-01T00:00:00Z